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    <!-- http://purl.obolibrary.org/obo/MONDO_0001083 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0001083">
        <rdfs:label>Fanconi renotubular syndrome</rdfs:label>
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        <rdfs:seeAlso rdf:datatype="http://www.w3.org/2001/XMLSchema#anyURI">https://rarediseases.info.nih.gov/diseases/9120/fanconi-syndrome</rdfs:seeAlso>
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        <oboInOwl:hasDbXref>MEDGEN:4653</oboInOwl:hasDbXref>
        <oboInOwl:id>MONDO:0001083</oboInOwl:id>
        <oboInOwl:hasRelatedSynonym>toni-debre-Fanconi syndrome</oboInOwl:hasRelatedSynonym>
        <oboInOwl:hasExactSynonym>Fanconi syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasExactSynonym>Lignac-Fanconi syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>SCTID:236466005</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>SCTID:40488004</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Fanconi-de toni syndrome</oboInOwl:hasExactSynonym>
        <ns5:IAO_0000115>A genetic or acquired disorder characterized by impairment of the function of the proximal tubules of the kidney. It results in decreased reabsorption of electrolytes, glucose, amino acids, and other nutrients.</ns5:IAO_0000115>
        <oboInOwl:hasDbXref>NANDO:2200187</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>NCIT:C3034</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>UMLS:C0015624</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>Fanconi&#39;s syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasNarrowSynonym>congenital Fanconi syndrome</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasDbXref>DOID:1062</oboInOwl:hasDbXref>
        <oboInOwl:hasExactSynonym>De toni-debre-Fanconi syndrome</oboInOwl:hasExactSynonym>
        <oboInOwl:hasDbXref>NANDO:2100027</oboInOwl:hasDbXref>
        <oboInOwl:hasNarrowSynonym>adult Fanconi syndrome</oboInOwl:hasNarrowSynonym>
        <oboInOwl:hasDbXref>MESH:D005198</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>icd11.foundation:788002727</oboInOwl:hasDbXref>
        <oboInOwl:hasDbXref>GARD:0009120</oboInOwl:hasDbXref>
        <oboInOwl:hasRelatedSynonym>infantile nephropathic cystinosis</oboInOwl:hasRelatedSynonym>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0002254 -->

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        <rdfs:label>syndromic disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0003847 -->

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        <rdfs:label>hereditary disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0006510 -->

    <Class rdf:about="http://purl.obolibrary.org/obo/MONDO_0006510">
        <rdfs:label>renal tubular transport disease</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/MONDO_0021568 -->

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        <rdfs:label>renal tubule disorder</rdfs:label>
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    <!-- http://purl.obolibrary.org/obo/UBERON_0001287 -->

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        <rdfs:label>proximal convoluted tubule</rdfs:label>
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